Project Lyme hosts regular educational, awareness, and fundraising events covering topic areas critical to our community.
May 08, 2025
Project Lyme is proud to provide a platform to support men who have been affected by Lyme disease and associated infections. The Men's Support Group involves regular virtual meet-ups via Zoom. Participants will discuss a common theme at each meeting, share stories of their own struggles caused by Lyme, and hear advice from other men going through the same things as them. Join us by registering through the links above!
June 07, 2025
The International Lyme and Associated Diseases Society (ILADS) in partnership with PA Lyme Resource Network invites healthcare professionals to join us for a two-day conference covering the latest clinical treatments and research updates for Lyme and other tick-borne illnesses.
January 23, 2025
This event will provide an educational presentation, coping strategies workshop, resource sharing, and a supportive Q&A session. The event will serve as a meaningful step towards raising awareness and providing support for Lyme patients, highlighting the vital connection between physical and emotional well-being.
January 22, 2025
Center for Lyme Action will host its annual Virtual Fly-In to connect advocates with their Members of Congress. Last year 350 advocates registered for more than 200 meetings with Congress Members.
January 22, 2025
This event is designed to provide a foundational understanding of babesiosis and Tafenoquine’s clinical development program in Babesiosis, a tick-borne parasitic infection, which poses a growing health concern in many regions.
November 20, 2024
The goal of this webinar is to teach patients how to effectively advocate for change on the Federal, State, and local levels of government. Our presenters will discuss multiple topics including but not limited to: ways to engage with political representatives through letter writing, proclamation requests, how to participate in the upcoming Center for Lyme Action Fly-In and how to advocate for change hyper-locally, such as planning 5k's, social media fundraisers.
November 19, 2024
Illness invalidation, by medical professionals or others, is a common experience for patients with Lyme disease. This talk will discuss recent scientific articles in Lyme and other illnesses about the patient effects of invalidation. It will also discuss the gendered history of invalidation and how it influences the medical encounter today.
November 14, 2024
The goal of this webinar is to teach patients how to effectively advocate for change on the Federal, State, and local levels of government. Our presenters will discuss multiple topics including but not limited to: ways to engage with political representatives through letter writing, proclamation requests, how to participate in the upcoming Center for Lyme Action Fly-In and how to advocate for change hyper-locally, such as planning 5k's, social media fundraisers.